Article Versions Notes

Peixoto de Barcelos I, Li D, Watson D, M. McCormick E, Elden L, Aleman TS, O’Neil EC, J. Falk M, Hakonarson H. Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient. Brain Sciences. 2023; 13(8):1210. https://doi.org/10.3390/brainsci13081210

Peixoto de Barcelos, Isabella, Dong Li, Deborah Watson, Elizabeth M. McCormick, Lisa Elden, Thomas S. Aleman, Erin C. O’Neil, Marni J. Falk, and Hakon Hakonarson. 2023. "Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient" Brain Sciences 13, no. 8: 1210. https://doi.org/10.3390/brainsci13081210

Peixoto de Barcelos, I., Li, D., Watson, D., M. McCormick, E., Elden, L., Aleman, T. S., O’Neil, E. C., J. Falk, M., & Hakonarson, H. (2023). Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient. Brain Sciences, 13(8), 1210. https://doi.org/10.3390/brainsci13081210